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rs746446116

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs746446116(A;G)
Make rs746446116(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position18018634
GeneATPAF2
is asnp
is mentioned by
dbSNPrs746446116
ebirs746446116
HLIrs746446116
Exacrs746446116
Varsomers746446116
Maprs746446116
PheGenIrs746446116
hapmaprs746446116
1000 genomesrs746446116
hgdprs746446116
ensemblrs746446116
gopubmedrs746446116
geneviewrs746446116
scholarrs746446116
googlers746446116
pharmgkbrs746446116
gwascentralrs746446116
openSNPrs746446116
23andMers746446116
23andMe allrs746446116
SNP Nexus

SNPshotrs746446116
SNPdbers746446116
MSV3drs746446116
GWAS Ctlgrs746446116
Max Magnitude0
ClinVar
Risk rs746446116(G;G)
Alt rs746446116(G;G)
Reference Rs746446116(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ATPAF2
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.17921948A>G
CLNSRC
CLNACC RCV000200702.1,